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    • 77. 发明授权
    • Substituted dioxolan and dioxan derivatives useful as pesticides
    • US4971981A
    • 1990-11-20
    • US145432
    • 1988-01-19
    • Friedrich Karrer
    • Friedrich Karrer
    • C07D317/18A01N43/28A01N43/30A01N43/32A01N43/40A01N47/12C07D317/22C07D317/50C07D317/54C07D317/64C07D317/72C07D319/12C07D319/14C07D319/16C07D405/04C07D407/04C07D409/04
    • C07D405/04A01N43/28A01N43/30A01N43/32A01N43/40A01N47/12C07D317/22C07D317/64C07D317/72C07D319/12C07D407/04C07D409/04
    • Novel substituted 1,3-dioxolan and 1,4-dioxan derivatives of formula I ##STR1## in which R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 each independently of the others represents hydrogen or C.sub.1 -C.sub.4 -alkyl or, if n=1,R.sub.2 and R.sub.4 together represent one of the radicals ##STR2## R.sub.7 represents hydrogen, halogen, methyl, ethyl, C.sub.1 -C.sub.2 -alkyl substituted by 1 to 5 halogen atoms, methoxy, ethoxy or C.sub.1 -C.sub.2 -alkoxy substituted by 1 to 5 halogen atoms;R.sub.8 represents a halogen, C.sub.1 -C.sub.3 -alkyl, C.sub.1 -C.sub.3 -alkyl substituted by 1 to 7 halogen atoms, C.sub.1 -C.sub.3 -alkoxy, C.sub.1 -C.sub.3 -alkoxy substituted by 1 to 7 halogen atoms, or cyano;U represents a grouping --CH.dbd. or --N.dbd.;X represents --O--, --S-- or --N(R.sub.9)--;Y represents --O--, --S--, --S(O)--, --S(O.sub.2)--, --CH.sub.2 --, --CO-- or --N(R.sub.9)--, whereinR.sub.9 represents hydrogen, C.sub.1 -C.sub.4 -alkyl or alkylcarbonyl having a total of from 2 to 4 carbon atoms;n is a number 0 or 1;m is a number 0, 1 or 2;p is a number 1, 2 or 3; andZ represents one of the radicals ##STR3## wherein R.sub.10 represents hydrogen, methyl or ethyl;R.sub.11 represents hydrogen, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.2 -C.sub.4 -alkenyl, C.sub.2 -C.sub.4 -alkynyl, alkoxyalkyl having a total of 2 to 6 carbon atoms, C.sub.1 -C.sub.6 -alkyl substituted by 1 to 7 halogen atoms, benzyl or benzyl substituted in the nucleus by a halogen atom, by a C.sub.1 -C.sub.3 -alkyl radical or by a C.sub.1 -C.sub.3 -alkoxy radical, cyanomethyl, (C.sub.1 -C.sub.2 -alkoxy)-carbonyl or the radical --CH.sub.2 --NH--COO--(C.sub.1 -C.sub.2 -alkyl);R.sub.12 represents hydrogen, C.sub.1 -C.sub.6 -alkyl, phenyl, phenyl substituted by 1 to 3 substituents from the group consisting of halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.3 -alkyl substituted by 1 to 7 halogen atoms, C.sub.2 -C.sub.4 -alkenyl, C.sub.2 -C.sub.4 -alkynyl, C.sub.1l -C.sub.3 -alkoxy, C.sub.1 -C.sub.3 -alkoxy substituted by from 1 to 7 halogen atoms, alkoxyalkyl having a total of from 2 to 5 carbon atoms, C.sub.3 -C.sub.4 -alkenyloxy, C.sub.3 -C.sub.4 -alkynyloxy and C.sub.1 -C.sub.3 -alkylthio, or represents pyridyl, furan-2-yl, thien-2-yl or the radical ##STR4## R.sub.12 and R.sub.11 together represent one of the groups ##STR5## and R.sub.13 and R.sub.14 each independently of the other represents hydrogen, halogen or C.sub.1 -C.sub.3 -alkyl; orR.sub.13 and R.sub.14 together represent the group ##STR6## Processes for the preparation of these compounds and their use in pest control, especially for controlling insects and representatives of the order Acarina, are described.
    • 79. 发明授权
    • Nonanol/nonene antimicrobial compositions
    • 壬醇/壬烯抗菌组合物
    • US4803290A
    • 1989-02-07
    • US55645
    • 1987-05-29
    • Basil A. BurkeMuraleedharan Nair
    • Basil A. BurkeMuraleedharan Nair
    • A01N43/30C07D317/50C07D317/54
    • A01N43/30C07D317/50
    • Substituted 5'-nonanol/5'-nonene compounds which exhibit important antimicrobial and antifungal activity, compositions and methods of delivery against pathovars and pathogens, and methods of synthesis from commonly available reactants. The antimicrobial composition active ingredient is one or more substituted 1,2-alkylidenedioxybenzene compounds of the formula: ##STR1## where R.sub.3 is selected from 5'-nonanol and 5'-nonene, and R.sub.1 and R.sub.2 are selected from H and C.sub.1 -C.sub.5 alkyl, alkenyl and alkynyl groups. The preferred compounds are 5-(5'-hydroxy- 5'- nonanyl)-1,1-methylenedioxybenzene and 4-(5'-non-4'-enyl)-1,2-methylenedioxybenzene. Compositions including these compounds exhibit antimicrobial activity against a variety of pathogens and pathovars, e.g., Xanthomonas campestris spp. bacteria, antifungal activity against a variety of fungi and bacteria, and are highly specific, e.g., having antifungal activity against wheat powdery mildew and cucumber downy mildew, but do not affect seed germination or have appreciable herbicidal or insecticidal activity. Methods and compositions for delivery of these agents against such pathogens, and methods of chemical synthesis of the compounds are disclosed.
    • 表现出重要的抗微生物和抗真菌活性的替代的5'-壬醇/ 5'-壬烯化合物,对病原体和病原体递送的组合物和方法,以及通常可得到的反应物的合成方法。 抗微生物组合物活性成分是一种或多种下式的取代的1,2-亚烷基二氧基苯化合物:其中R 3选自5'-壬醇和5'-壬烯,并且R 1和R 2选自H和C 1 -C 5 烷基,烯基和炔基。 优选的化合物是5-(5'-羟基-5'-壬酰基)-1,1-亚甲二氧基苯和4-(5'-非-4'-烯基)-1,2-亚甲二氧基苯。 包括这些化合物的组合物对各种病原体和病原体表现出抗菌活性,例如野油菜黄单胞菌(Xanthomonas campestris spp。) 细菌,针对各种真菌和细菌的抗真菌活性,并且高度特异性,例如对小麦白粉病和黄瓜霜霉病具有抗真菌活性,但不影响种子萌发或具有明显的除草或杀虫活性。 公开了用于递送这些试剂以抵抗这种病原体的方法和组合物,以及化合物的化学合成方法。